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Comment: Comment: 99.9999% of Q30 bases is normal?
21 days ago by MatthewP ★ 1.4k
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1
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413
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Comment: Comment: A c library for reading and writing sequences in fasta and fastq format.
8 weeks ago by MatthewP ★ 1.4k
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2
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1.3k
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Comment: Comment: Some lines are not well organized in BED file, how to correct them ? Thanks a lo
3 months ago by MatthewP ★ 1.4k
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0
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2.4k
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Comment: Comment: Should I use the basecaller Dorado to analyze my Nanopore Data?
4 months ago by MatthewP ★ 1.4k
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0
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413
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Comment: Comment: MSA using ggtree msaplot
4 months ago by MatthewP ★ 1.4k
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0
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510
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Comment: Comment: ANNOVAR Error: All variants in a VCF register as "invalid genotype records in in
5 months ago by MatthewP ★ 1.4k
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1
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510
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Comment: Comment: ANNOVAR Error: All variants in a VCF register as "invalid genotype records in in
5 months ago by MatthewP ★ 1.4k
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0
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811
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Comment: Comment: What is the new Entrez login for NCBI API?
6 months ago by MatthewP ★ 1.4k
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0
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542
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Comment: Comment: How to deal with reads which CIGAR is [0-9]+S
6 months ago by MatthewP ★ 1.4k
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0
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551
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Comment: Comment: What is a tool to get the genome build of a VCF?
6 months ago by MatthewP ★ 1.4k
1
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1
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858
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Comment: Comment: how to solve the problem "Invalid character (+) in sequence"
8 months ago by MatthewP ★ 1.4k
1
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1
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888
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Comment: Comment: How to make chromVAR plot?
9 months ago by MatthewP ★ 1.4k
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1
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1.0k
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Comment: Comment: All question mark quality scores on several studies
10 months ago by MatthewP ★ 1.4k
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1
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1.0k
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Comment: Comment: All question mark quality scores on several studies
10 months ago by MatthewP ★ 1.4k
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0
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1.1k
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Comment: Comment: OTU, ASV and Kraken2
10 months ago by MatthewP ★ 1.4k
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1
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1.0k
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Comment: Comment: All question mark quality scores on several studies
10 months ago by MatthewP ★ 1.4k
0
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1
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1.6k
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Comment: Comment: End to End Solution for Multiple Sequence Alignment on Fasta Files in Python
10 months ago by MatthewP ★ 1.4k
1
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0
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421
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Comment: Comment: weird behaviour on bedtools
11 months ago by MatthewP ★ 1.4k
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0
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683
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Comment: Comment: Comparing variant calls
12 months ago by MatthewP ★ 1.4k
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1
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3.0k
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Comment: Comment: gseKEGG - no gene can be mapped (RNAseq analysis)
14 months ago by MatthewP ★ 1.4k
0
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1
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1.5k
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Comment: Comment: R:scheduled cores 1, 5 did not deliver results
14 months ago by MatthewP ★ 1.4k
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0
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2.6k
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Comment: Comment: MSA visualization python package for sequence analysis
17 months ago by MatthewP ★ 1.4k
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0
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769
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Comment: Comment: How can Biostrings calculate consensus sequence without counting gaps?
18 months ago by MatthewP ★ 1.4k
2
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1
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805
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Comment: Comment: HISAT2 running issue (output getting slower)
19 months ago by MatthewP ★ 1.4k
0
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1
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1.6k
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Comment: Comment: Set up conda rna seq analysis
22 months ago by MatthewP ★ 1.4k
0
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1
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1.6k
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Comment: Comment: Set up conda rna seq analysis
22 months ago by MatthewP ★ 1.4k
1
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1
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1.6k
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Comment: Comment: bowtie2 error "Unable to read file magic number"
22 months ago by MatthewP ★ 1.4k
0
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0
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992
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Comment: Comment: How to handle 2 peaks in fastQC GC plot...
23 months ago by MatthewP ★ 1.4k
0
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0
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950
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Comment: Comment: featureCounts stuck
2.1 years ago by MatthewP ★ 1.4k
0
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1
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1.6k
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Comment: Comment: How to do pathway enrichment analysis with genomic ranges data (ATAC-Seq peaks)?
2.2 years ago by MatthewP ★ 1.4k
1
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0
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3.0k
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Comment: Comment: DiffBind missing peaks and FRiP
2.2 years ago by MatthewP ★ 1.4k
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0
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1.7k
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Comment: Comment: Bedtools genomecov - Bam to bedgraph conversion
2.4 years ago by MatthewP ★ 1.4k
0
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1
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1.5k
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Comment: Comment: Best practice for running GATK VQSR on X chromosome
2.5 years ago by MatthewP ★ 1.4k
0
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1
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1.7k
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Comment: Comment: featureCounts low annotation rate RNA-seq
2.5 years ago by MatthewP ★ 1.4k
0
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1
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1.7k
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Comment: Comment: featureCounts low annotation rate RNA-seq
2.5 years ago by MatthewP ★ 1.4k
1
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0
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1.2k
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Comment: Comment: quick way of contamination identification from fastq file
2.9 years ago by MatthewP ★ 1.4k
0
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1
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892
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Comment: Comment: Normalisation of RNA-seq data for coexpression analysis
2.9 years ago by MatthewP ★ 1.4k
0
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0
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715
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Comment: Comment: Troubleshooting: rRNA depletion RNAseq no DE genes
3.0 years ago by MatthewP ★ 1.4k
0
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0
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2.7k
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Comment: Answer: Installing SRAToolKit
3.1 years ago by MatthewP ★ 1.4k
0
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0
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5.6k
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Comment: Comment: How to do Disease-Free survival analysis with TCGA data ??
3.1 years ago by MatthewP ★ 1.4k
0
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0
replies
1.7k
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Comment: C: Downloading 1000genome phase 3 data in 38 build
3.2 years ago by MatthewP ★ 1.4k
0
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1
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892
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Comment: C: About shell script
3.2 years ago by MatthewP ★ 1.4k
0
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0
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2.9k
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Comment: C: Bowtie2 command does not produce output file
3.3 years ago by MatthewP ★ 1.4k
1
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0
replies
5.8k
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Comment: C: How to create interval list from reference fasta or dict file?
3.3 years ago by MatthewP ★ 1.4k
1
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0
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5.8k
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Comment: C: How to create interval list from reference fasta or dict file?
3.3 years ago by MatthewP ★ 1.4k
0
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1
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931
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Comment: C: How to get gene level of differential expression from 2 color channel array with
3.3 years ago by MatthewP ★ 1.4k
0
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1
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931
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Comment: C: How to get gene level of differential expression from 2 color channel array with
3.3 years ago by MatthewP ★ 1.4k
1
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1
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2.8k
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Comment: C: About GATK4 Mutect2 runtime (Whole Exome seq)
3.3 years ago by MatthewP ★ 1.4k
0
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1
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1.2k
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Comment: C: How to analysis 2 color microarray data from GEO with limma?
3.3 years ago by MatthewP ★ 1.4k
0
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0
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1.4k
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Comment: C: SNPs in Promoter region
3.3 years ago by MatthewP ★ 1.4k
148 results • Page 1 of 3
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